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Determination of Se and Te in coal at ultra-trace levels by ICP-MS after microwave-induced combustion

机译:微波诱导燃烧后ICP-MS测定超痕量煤中的硒和碲

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A method for ultra-trace determination of Se and Te in coal by inductively coupled plasma mass spectrometry (ICP-MS) was developed. Samples (up to 500 mg) were prepared by microwave-induced combustion (MIC) in a closed system pressurized with 20 bar of oxygen. Inorganic acids or their mixtures were evaluated as absorbing solution. Using HNO3 + HCl (1 + 1), results obtained for Se and Te after sample preparation by MIC agreed with those obtained by reference methods, microwave-assisted wet digestion (MAWD) using concentrated HNO3 and HF, and solid sampling electrothermal vaporization inductively coupled plasma mass spectrometry (SS-ETV-ICP-MS), and also with a certified reference material of coal (NIST 1632c) for Se. Very low limits of quantification (LOQ) were obtained: 0.002 and 0.007 mg kg(-1) for Se and Te, respectively. Major elements were determined in final solutions obtained by MAWD and MIC, and their concentration in solutions of MIC was negligible (<10 mu g L-1), minimizing the risk of interference in ICP-MS analysis. The proposed method was applied to samples of coal from the United Kingdom, with a wide range of inorganic composition (from 3 to 41% ash content), showing its robustness and feasibility for routine analysis. Se concentration ranged from 0.291 to 11.5 mg kg(-1), and Te was mainly found at ultra-trace levels (<0.007 to 0.11 mg kg(-1)). The proposed method presents several advantages over the reference methods, such as the use of a higher sample mass, low LOQs and, an important aspect, no need of using HF.
机译:建立了电感耦合等离子体质谱法(ICP-MS)超痕量测定煤中硒和碲的方法。在密闭系统中用20 bar氧气加压,通过微波诱导燃烧(MIC)制备样品(最多500 mg)。无机酸或其混合物被评估为吸收溶液。使用HNO3 + HCl(1 + 1),通过MIC制备样品后获得的Se和Te的结果与参考方法,使用浓HNO3和HF的微波辅助湿消解(MAWD)以及电感耦合的固体样品电热汽化的结果相符。等离子体质谱法(SS-ETV-ICP-MS),还使用经过认证的煤炭标准物质(NIST 1632c)作为硒。获得了非常低的定量限(LOQ):Se和Te分别为0.002和0.007 mg kg(-1)。在由MAWD和MIC获得的最终溶液中确定了主要元素,并且它们在MIC溶液中的浓度可以忽略不计(<10μg L-1),从而将ICP-MS分析中的干扰风险降至最低。所提出的方法应用于来自英国的煤样品,该样品具有广泛的无机成分(灰分含量从3%到41%),显示了其鲁棒性和常规分析的可行性。 Se的浓度范围为0.291至11.5 mg kg(-1),而Te主要以超痕量水平(<0.007至0.11 mg kg(-1))发现。与参考方法相比,所提出的方法具有多个优点,例如,使用更高的样品质量,较低的LOQ,并且一个重要方面是无需使用HF。

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